Book a demo

"*" indicates required fields

This field is for validation purposes and should be left unchanged.

Access your download

Fill in your details to get instant access to this resource.

"*" indicates required fields

This field is for validation purposes and should be left unchanged.

About AB Cube Germany

Innovating Clinical Trials
Since 2002

We are a proud part of the AB Cube Group. Our offering provides an innovative End-to-End eClinical solution that meets growing customer demands across clinical operations and clinical data management through its integrated suite of applications.

We bring over 20 years of experience with EDC software. Our employees are experts in clinical research, project management, software development, data privacy and data security. With fast response times, we are focused on your trial.

We believe that every day saved can make a difference.
The company was founded in Munich, Germany with a vision to build a new EDC system leveraging CDISC standards to accelerate the database build and reduce data management programming efforts.

2002

XClinical was founded in Munich

2003

Marvin EDC

Launch of Marvin EDC

2007

Marvin 2.0 will be one of the first EDC systems to be CDISC certified

2013

First oncology registry with sub-studies in Marvin

2020

Marvin EDC

Marvin 3.0 released

2023

ODSeasyNet

Asthenis software for documenting cancer cases joins with Marvin

2024

Marvin EDC

Release and onboarding of our Data Hub and Reporting Module “StudyMetrIQs”

2025

Study Designer (AI-enabled)

Release of first AI Use Cases

2026

Merger & Acquisition

Merger and acquistion with AB Cube. Integrating with Vigilance Suite from AB Cube SafetyEasy®

Why Marvin & AB Cube?

Purpose-Built for Complex Clinical Trials
Vast Trial & Oncology Experience
Highly Configurable
CDISC-Native
Adaptive & Complex Trial Designs
Cost-Effective vs. Global Players
Full Control to Customize Workflows and Fields

Compliance & Security by Design - Built on a robust, pre-validated framework aligned with GCP and 21 CFR Part 11 Standards.

Full Compliance with GCP and 21 CFR Part 11 Standards

Our solutions provide complete compliance with Good Clinical Practice (GCP) and 21 CFR Part 11, featuring secure eSignatures and audit trails that simplify regulatory audits and enhance research credibility.

GDPR-Compliant Data Handling and EU Data Storage

We host data securely within the EU, ensuring compliance with GDPR standards for academic institutions in Europe and securing sensitive patient data with SSL encryption.

Secure Audit Trails and Role-Based Access

Maintain detailed audit trails for transparency and role-based access control to safeguard against unauthorized access, ensuring that only approved personnel handle sensitive information.

Fast Facts About AB Cube

25+ Years of Innovation

Pioneering EDC since 2002.

30+ Countries Served

A trusted global partner in pharmacovigilance, medical device vigilance, cosmetovigilance, and nutrivigilance.

10,000+ Trials conducted

Trials conducted across oncology, neurology, cardiology & rare disease

500+ Sites

Relationships with more than 500 oncology and cancer center sites globally

100% Cloud-Based

No local installation, no maintenance hassle.

AI enabler

Integration of future ready solutions enabled by AI with a strong focus on data safety and integrity